JPH05225989A - Manufacture of thin type battery - Google Patents

Manufacture of thin type battery

Info

Publication number
JPH05225989A
JPH05225989A JP4061213A JP6121392A JPH05225989A JP H05225989 A JPH05225989 A JP H05225989A JP 4061213 A JP4061213 A JP 4061213A JP 6121392 A JP6121392 A JP 6121392A JP H05225989 A JPH05225989 A JP H05225989A
Authority
JP
Japan
Prior art keywords
active material
sealing agent
current collector
paper
holes
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP4061213A
Other languages
Japanese (ja)
Inventor
Hiroshi Kagawa
博 香川
Shiro Kato
史朗 加藤
Kazuo Murata
和雄 村田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Yuasa Corp
Original Assignee
Yuasa Corp
Yuasa Battery Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Yuasa Corp, Yuasa Battery Corp filed Critical Yuasa Corp
Priority to JP4061213A priority Critical patent/JPH05225989A/en
Priority to CA002107470A priority patent/CA2107470A1/en
Priority to PCT/JP1993/000159 priority patent/WO1993016497A1/en
Priority to US08/122,569 priority patent/US5431701A/en
Priority to EP93903327A priority patent/EP0581964B1/en
Priority to DE69319389T priority patent/DE69319389T2/en
Publication of JPH05225989A publication Critical patent/JPH05225989A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M6/00Primary cells; Manufacture thereof
    • H01M6/04Cells with aqueous electrolyte
    • H01M6/06Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid
    • H01M6/12Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid with flat electrodes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/04Construction or manufacture in general
    • H01M10/0436Small-sized flat cells or batteries for portable equipment
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50Manufacturing or production processes characterised by the final manufactured product
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/49002Electrical device making
    • Y10T29/49108Electric battery cell making
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/49002Electrical device making
    • Y10T29/49108Electric battery cell making
    • Y10T29/4911Electric battery cell making including sealing

Landscapes

  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Primary Cells (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

PURPOSE:To achieve enhancement of the productivity and stabilization of the product quality, by providing holes for an active material in a sealant sheet on a metallic current collector, and causing retention of the active material, electrolyte, etc., and then peeling off the sealant sheet. CONSTITUTION:A metallic current collector 1 is adhered onto a base paper A, and a sealant sheet 2 consisting of a polyethylene resin is adhered on the current collector 1. Next, active material retention holes are provided in the sealant sheet 2, and a positive electrode activator 4 is coated thereon, and desiccated and crosslinked. Subsequently, a base paper B is peeled off, and a base paper C consisting of polypropylene resin and provided thereon with an exfoliation paper 5 is adhered. The resulting sheet is formed with holes 6 into which an electrolyte 7 is coated, and desiccated and crosslinked. Next, the exfoliation paper 5 of the base paper C is removed, after which a base paper D consisting of a polypropylene resin and provided thereon with an exfoliation paper 8 is adhered and holes 9 are formed therein. A negative electrode activator 10 is transferred and the exfoliation paper 8 is removed. Subsequently, a metallic current collector 11 is disposed and then thermal compression bonding is effected under vacuumized condition to seal the sealant 2.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、エレクトロニクス機
器、電気自動車などの分野に使われる薄形電池の製造方
法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for manufacturing a thin battery used in fields such as electronic equipment and electric vehicles.

【0002】[0002]

【従来の技術】従来この種の薄形電池の製造は、図4に
示すような電池構造において、集電体の表面に型枠をお
いて活物質を塗布し、次に活物質の周囲に封口剤を配置
し、このようにして作製した各集電体を重ねることで薄
形電池を製造していた。
2. Description of the Related Art Conventionally, in the manufacture of a thin battery of this type, in a battery structure as shown in FIG. 4, an active material is applied on the surface of a current collector with a frame, and then the active material is surrounded. A thin battery was manufactured by disposing a sealing agent and stacking the respective current collectors thus manufactured.

【0003】[0003]

【発明が解決しようとする課題】このような従来の製造
方法では量産が困難である上に品質(塗布厚さ、塗布領
域・面積など)にばらつきがあった。本発明は、上記の
問題点に鑑みなされたもので、電池製造能力の向上と品
質安定を計る製造方法を提供することを目的とするもの
である。
With such a conventional manufacturing method, mass production is difficult and quality (coating thickness, coating area / area, etc.) varies. The present invention has been made in view of the above problems, and an object of the present invention is to provide a manufacturing method that improves battery manufacturing capacity and stabilizes quality.

【0004】[0004]

【課題を解決するための手段】本発明は上記目的を達成
するべく、金属製集電体の表面に封口剤からなるシ−ト
層を設ける第1工程、該封口剤シ−ト層にハ−フカット
などにより活物質用の穴を設ける第2工程、該穴に活物
質、電解質などを保持する第3工程、前記ハ−フカット
済封口剤シ−トを取り除く第4工程などからなること、
前記金属性集電体が箔または蒸着膜で形成され、厚さが
0.001mm〜0.05mmであり、台紙が貼られて
いること、前記封口剤シ−トの片面に台紙が貼られてい
ること、前記活物質、電解質などを封口剤シ−トの穴に
保持させ、乾燥後に該活物質、電解質などの厚さが封口
剤の厚さとほぼ同等にすることなどを特徴とするもので
ある。
In order to achieve the above object, the present invention provides a first step of providing a sheet layer made of a sealing agent on the surface of a metal current collector, which is a step for coating the sealing agent sheet layer. -A second step of forming a hole for an active material by fucating or the like, a third step of holding the active material, the electrolyte or the like in the hole, a fourth step of removing the halfcutted sealing agent sheet, and the like,
The metallic current collector is formed of a foil or a vapor deposition film, has a thickness of 0.001 mm to 0.05 mm, and has a backing sheet attached, and the backing sheet is attached to one side of the sealing agent sheet. That the active material, the electrolyte, etc. are held in the holes of the sealing agent sheet, and the thickness of the active material, electrolyte, etc. after drying is substantially the same as the thickness of the sealing agent. is there.

【0005】[0005]

【作用】本発明において、箔または蒸着膜からなる金属
集電体表面に台紙A及び封口剤からなるシ−ト層を設け
ることにより該金属集電体表面の汚れを防止し、電池の
性能品質を向上させる。封口剤シ−トに台紙Bを貼るこ
とにより活物質を保持(塗布などによる)する際の封口
剤表面の汚れを防止し電池の密封性能を向上させる。封
口剤シ−ト層にハ−フカットなどにより台紙Bの上から
活物質用の穴を設けることにより活物質領域を一定にす
る。また封口剤シ−トの台紙Bの厚さは塗布された活物
質、電解質などの乾燥による収縮厚さにほぼ相当させる
効果を併せ持ち、次工程(例えば電解質塗布工程)の塗
布を容易にさせる。また金属性集電体が箔または蒸着膜
で厚さを0.001mm〜0.05mmとして台紙Aを
貼ることによりロ−ルなどで巻き取ることが容易とな
り、また柔軟性を向上させることから折り曲げにも強く
高速処理できる。
In the present invention, by providing a sheet layer composed of the mount A and the sealing agent on the surface of the metal current collector made of the foil or the vapor-deposited film, the surface of the metal current collector can be prevented from being contaminated and the performance of the battery Improve. By attaching the backing sheet B to the sealing agent sheet, the surface of the sealing agent is prevented from being soiled when the active material is held (by coating or the like), and the sealing performance of the battery is improved. The active material region is made constant by forming holes for the active material from the top of the mount B by means of half cut in the sealing agent sheet layer. The thickness of the mount sheet B of the sealing agent sheet also has the effect of making the applied active material, the electrolyte, etc., have a thickness substantially equivalent to the contracted thickness due to drying, and facilitates the application in the next step (eg, the electrolyte application step). Further, the metallic current collector is a foil or a vapor-deposited film having a thickness of 0.001 mm to 0.05 mm, and by attaching the backing sheet A, it becomes easy to wind it by a roll or the like, and the flexibility is improved. It can process at high speed.

【0006】[0006]

【実施例】以下、本発明の詳細について、一実施例によ
り説明する。図1に示すように幅が約400mmのポリ
プロピレン系樹脂からなる台紙A(厚さは約0.1m
m)上にステンレス箔(幅;300mm、厚さ;0.0
2mm)からなる金属集電体1を接着し、さらに金属集
電体1面に上面にポリエチレン系樹脂からなる剥離紙B
(幅;約300mm、厚さ;約0.01mm)が接着さ
れたポリプロピレン系樹脂からなる封口剤2シ−ト
(幅;約300mm、厚さ;約0.05mm)を接着し
た。以上が第1工程に相当する。次に封口剤2をハ−フ
カットにより活物質保持用の穴3を設けた。以上が第2
工程に相当する。さらに該穴3にドクタ−コ−タ−によ
り正極活物質4を約0.06mm厚さで塗布した。次に
約100℃〜約250℃で乾燥した。この時、正極活物
質4の厚さは約20%収縮し、約0.05mmとなっ
た。続いて電子線照射により架橋した。次に台紙Bを剥
離し、続いて上面に剥離紙5を設けたポリプロピレン系
樹脂からなる台紙C(幅;約300mm、厚さ;約0.
02mm)をその上から接着した。さらにハ−フカット
により台紙Cに穴3より大きい穴6を設けた。続いて電
解質7を該穴6にドクタ−コ−タ−により塗布した。乾
燥後、電子線照射により架橋した。次に台紙Cの剥離紙
5を取り除いた後、再び剥離紙8を設けたポリプロピレ
ン系樹脂からなる台紙D(幅;約300mm、厚さ;約
0.02mm)を接着した。次に再びハ−フカットによ
り台紙Dに穴3とほぼ等しい穴9を設けた。さらに別の
工程でハ−フカットされた負極活物質10を該穴9に転
写した。続いて剥離紙8を取り除いた後、第1工程と同
様に製造された金属集電体11(外表面に台紙Aが接着
されている。)を配置し、減圧下で熱圧着し封口剤2、
台紙C、台紙D(なお金属集電体11の内面にあらかじ
め封口剤が接着されていてもよい。)により電池内を減
圧密封した。次に電池の外周(少し台紙Aの外周を残し
て)をハ−フカットした。
EXAMPLES Details of the present invention will be described below with reference to examples. As shown in FIG. 1, a mount A made of polypropylene resin with a width of about 400 mm (thickness is about 0.1 m
m) on top of stainless steel foil (width: 300 mm, thickness: 0.0
2 mm) of the metal current collector 1 is adhered, and the release paper B made of polyethylene resin is attached to the surface of the metal current collector 1 on the upper surface.
2 sheets (width: about 300 mm, thickness: about 0.05 mm) of a sealing agent made of polypropylene resin to which (width: about 300 mm, thickness: about 0.01 mm) were adhered. The above corresponds to the first step. Next, the sealing agent 2 was half cut to form the holes 3 for holding the active material. The above is the second
It corresponds to a process. Further, a positive electrode active material 4 having a thickness of about 0.06 mm was applied to the hole 3 with a doctor coater. It was then dried at about 100 ° C to about 250 ° C. At this time, the thickness of the positive electrode active material 4 contracted by about 20% to about 0.05 mm. Then, it was cross-linked by electron beam irradiation. Next, the mount B is peeled off, and then the mount C made of polypropylene resin having the release paper 5 on the upper surface (width: about 300 mm, thickness: about 0.
02 mm) was glued from above. Further, a hole 6 larger than the hole 3 was formed in the mount C by half cut. Subsequently, the electrolyte 7 was applied to the holes 6 with a doctor coater. After drying, it was crosslinked by electron beam irradiation. Next, the release paper 5 of the mount C was removed, and then the mount D (width: about 300 mm, thickness: about 0.02 mm) made of polypropylene resin provided with the release paper 8 was adhered again. Next, a hole 9 which is almost the same as the hole 3 is formed in the mount D again by half cut. Further, the half-cut negative electrode active material 10 was transferred to the hole 9 in another step. Then, after removing the release paper 8, the metal current collector 11 (the backing sheet A is adhered to the outer surface) manufactured in the same manner as in the first step is arranged, and thermocompression-bonded under reduced pressure to obtain the sealing agent 2. ,
The inside of the battery was vacuum-sealed with a mount C and a mount D (a sealing agent may be adhered to the inner surface of the metal current collector 11 in advance). Next, the outer periphery of the battery (leaving the outer periphery of the mount A slightly) was half-cut.

【0007】このようにして得られた薄形電池12の斜
視図を図2に、図2のI−I部の拡大断面図を図3に示
す。この時、端子13、13’が上下に配置されてい
る。なおこの状態では端子13及び13’の片面に台紙
Aが接着しており、電気的短絡を防止している。
FIG. 2 is a perspective view of the thin battery 12 thus obtained, and FIG. 3 is an enlarged cross-sectional view taken along the line II of FIG. At this time, the terminals 13 and 13 'are arranged vertically. In this state, the mount A is adhered to one surface of the terminals 13 and 13 'to prevent an electrical short circuit.

【0008】従来の製造工程では電池生産数が最大30
セル/分であったのに対して、本発明では100セル/
分となり量産に対応した。また電池容量のバラツキ及び
製造時の不良率を表1に示した。
In the conventional manufacturing process, the maximum number of batteries produced is 30.
While the cell / minute was 100 cells / minute in the present invention.
This corresponds to mass production. In addition, Table 1 shows the variation in battery capacity and the defective rate during manufacturing.

【0009】 [0009]

【0010】さらに金属集電体の厚みを変えた場合の集
電体を順次加工する際のロ−ル送り時の曲げからくる気
密不良率と金属集電体の電圧降下値を表2に示した。
Further, Table 2 shows the airtight defective rate and the voltage drop value of the metal current collector due to bending during roll feeding when sequentially processing the current collector when the thickness of the metal current collector is changed. It was

【0011】 [0011]

【0012】表2から分かる如く、金属集電体の厚みと
して約0.001mm〜0.05mmの範囲にあること
が生産性及び電池性能の点で望ましい。
As can be seen from Table 2, the thickness of the metal current collector is preferably in the range of about 0.001 mm to 0.05 mm from the viewpoint of productivity and battery performance.

【0013】[0013]

【発明の効果】上述したごとく、本発明は電池の生産性
(多量生産)を高め、電池性能向上を計るなど、従来に
比べて量産性及び信頼性が高く工業的価値は極めて大で
ある。
As described above, according to the present invention, the productivity (mass production) of the battery is improved and the battery performance is improved. Therefore, the mass productivity and the reliability are higher and the industrial value is extremely higher than the conventional one.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明の薄形電池の製造時の各工程の加工状態
経過を示す斜視図である。
FIG. 1 is a perspective view showing a process state progress of each step in manufacturing a thin battery of the present invention.

【図2】本発明の薄形電池の完成時の斜視図である。FIG. 2 is a perspective view of the thin battery of the present invention when it is completed.

【図3】図2のI−I部の拡大断面図である。FIG. 3 is an enlarged cross-sectional view of a II section in FIG.

【図4】従来の薄形電池の製造手順の斜視図である。FIG. 4 is a perspective view of a manufacturing procedure of a conventional thin battery.

【符号の説明】[Explanation of symbols]

1、11 金属集電体 2 封口剤 3、6、9穴 4 正極活物質 5、8 剥離紙 7 電解質 10 負極活物質 12 薄形電池 13 端子 13’ 端子 1, 11 Metal Current Collector 2 Sealant 3, 6, 9 Hole 4 Positive Electrode Active Material 5, 8 Release Paper 7 Electrolyte 10 Negative Electrode Active Material 12 Thin Battery 13 Terminal 13 'Terminal

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 正極活物質、電解質層及び負極活物質を
層状に重ねた発電要素からなる薄形電池の製造方法にお
いて、金属集電体の表面に封口剤からなるシ−ト層を設
ける第1工程、該封口剤シ−ト層にハ−フカットなどに
より活物質用の穴を設ける第2工程、該穴に活物質、電
解質などを保持する第3工程、前記ハ−フカット済封口
剤シ−トを取り除く第4工程からなることを特徴とする
薄形電池の製造方法。
1. A method for manufacturing a thin battery comprising a power generating element in which a positive electrode active material, an electrolyte layer and a negative electrode active material are layered, and a sheet layer made of a sealing agent is provided on the surface of a metal current collector. 1 step, 2nd step of forming holes for active material in the sealing agent sheet layer by half cut, etc., 3rd step of holding active material, electrolyte etc. in the holes, said half cut sealing agent sheet -A method of manufacturing a thin battery, comprising a fourth step of removing the battery.
【請求項2】 前記金属性集電体が箔または蒸着膜で形
成され、厚さが0.001mm〜0.05mmであり、
封口剤または剥離用の樹脂または紙からなる台紙が貼ら
れていることを特徴とする請求項1記載の薄形電池の製
造方法。
2. The metallic current collector is formed of a foil or a vapor deposition film and has a thickness of 0.001 mm to 0.05 mm,
The method for manufacturing a thin battery according to claim 1, wherein a mount made of a sealing agent, a peeling resin, or paper is attached.
【請求項3】 前記封口剤シ−トの片面に剥離用の樹脂
または紙からなる台紙が貼られていることを特徴とする
請求項1記載の薄形電池の製造方法。
3. The method of manufacturing a thin battery according to claim 1, wherein a mount made of resin or paper for peeling is attached to one surface of the sealing agent sheet.
【請求項4】 前記活物質、電解質を封口剤シ−トの穴
に保持させ、乾燥後に該活物質、電解質の厚さが封口剤
の厚さとほぼ同等にすることを特徴とする請求項1又は
3記載の薄形電池の製造方法。
4. The active material and the electrolyte are held in the holes of the sealing agent sheet, and the thickness of the active material and the electrolyte after drying is made substantially equal to the thickness of the sealing agent. Alternatively, the method for manufacturing the thin battery according to the above item 3.
JP4061213A 1992-02-14 1992-02-14 Manufacture of thin type battery Pending JPH05225989A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP4061213A JPH05225989A (en) 1992-02-14 1992-02-14 Manufacture of thin type battery
CA002107470A CA2107470A1 (en) 1992-02-14 1993-02-08 Manufacturing method of film type battery
PCT/JP1993/000159 WO1993016497A1 (en) 1992-02-14 1993-02-08 Method of producing thin cell
US08/122,569 US5431701A (en) 1992-02-14 1993-02-08 Manufacturing method of film type battery
EP93903327A EP0581964B1 (en) 1992-02-14 1993-02-08 Method of producing thin cell
DE69319389T DE69319389T2 (en) 1992-02-14 1993-02-08 METHOD FOR PRODUCING THIN CELLS

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4061213A JPH05225989A (en) 1992-02-14 1992-02-14 Manufacture of thin type battery

Publications (1)

Publication Number Publication Date
JPH05225989A true JPH05225989A (en) 1993-09-03

Family

ID=13164701

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4061213A Pending JPH05225989A (en) 1992-02-14 1992-02-14 Manufacture of thin type battery

Country Status (6)

Country Link
US (1) US5431701A (en)
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US9027242B2 (en) 2011-09-22 2015-05-12 Blue Spark Technologies, Inc. Cell attachment method
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CA2107470A1 (en) 1993-08-15
EP0581964B1 (en) 1998-07-01
EP0581964A1 (en) 1994-02-09
WO1993016497A1 (en) 1993-08-19
DE69319389T2 (en) 1998-10-29
US5431701A (en) 1995-07-11
DE69319389D1 (en) 1998-08-06
EP0581964A4 (en) 1995-12-06

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